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Does Routine Screening for Intimate Partner Violence Against Women in Health Care Settings do More Good Than Harm?

If, When and How to Ask the Question(s): Assessing Screening Approaches to Identifying Woman Abuse in Health Care Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00182468
Enrollment
5681
Registered
2005-09-16
Start date
2005-04-30
Completion date
2008-07-31
Last updated
2009-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intimate Partner Violence Against Women

Keywords

Domestic violence, Spouse Abuse

Brief summary

The purpose of the research is to evaluate whether routine screening for woman abuse in health care settings, as compared to no screening, does more good than harm. Recent reviews have identified the need for high quality research to understand 1) the actual impact on all women of instituting mass screening procedures to identify woman abuse and 2) the extent to which early identification through screening is effective in preventing or ameliorating important outcomes. The main outcomes for the study are reduction in violence, improvement in life quality, and potential harms of screening. A number of secondary outcomes to help understand the process by which screening and usual care might lead to changes in the primary outcomes will also be assessed.

Interventions

Women are screened for intimate partner violence prior to seeing a health care provider.

Sponsors

Echo: Improving Women's Health in Ontario (formerly Ontario Women's Health Council)
CollaboratorUNKNOWN
McMaster University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* Women aged 18-64 years * Patients at the health care site * Able to participate in English * Able to separate from accompanying person(s)

Exclusion criteria

* Too ill to participate * Unable to separate from accompanying person(s) * Unable to speak, read, or write English

Design outcomes

Primary

MeasureTime frame
Recurrence of intimate partner violence18 months
Health-specific quality of life18 months
Harms of screening and/or usual care18 months

Secondary

MeasureTime frame
Safety behaviours18 months
Use of information and resources18 months
Mental health (depression, post-traumatic stress disorder [PTSD], anxiety, somatic complaints, substance use)18 months
Stage in process of identifying and resolving abuse18 months
Exposure to maltreatment as a child18 months
Child quality of life18 months
Global physical and emotional health and well-being18 months
Health services utilization18 months

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026